Canonical Allele Identifier: CA348406092
Gene: PROC HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.128186301G>A (hg19) chr2:g.127428725G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428725G>A , CM000664.2:g.127428725G>A GRCh38
NC_000002.11:g.128186301G>A , CM000664.1:g.128186301G>A GRCh37
NC_000002.10:g.127902771G>A NCBI36
NG_016323.1:g.15306G>A , LRG_599:g.15306G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.1165G>A MANE Select ENSP00000234071.4:p.Gly389Ser
ENST00000234071.7:c.1165G>A ENSP00000234071.3:p.Gly389Ser
ENST00000402125.2:c.489G>A
ENST00000409048.1:c.1267G>A ENSP00000386679.1:p.Gly423Ser
NM_000312.3:c.1165G>A , LRG_599t1:c.1165G>A NP_000303.1:p.Gly389Ser
XM_005263715.3:c.1348G>A XP_005263772.1:p.Gly450Ser
XM_005263716.3:c.1330G>A XP_005263773.1:p.Gly444Ser
XM_005263717.3:c.1228G>A XP_005263774.1:p.Gly410Ser
XR_923313.1:n.1332-461C>T
XM_005263717.4:c.1228G>A XP_005263774.1:p.Gly410Ser
XM_017004505.1:c.1408G>A XP_016859994.1:p.Gly470Ser
XM_024453002.1:c.1510G>A XP_024308770.1:p.Gly504Ser
XM_024453003.1:c.1450G>A XP_024308771.1:p.Gly484Ser
XM_024453004.1:c.1348G>A XP_024308772.1:p.Gly450Ser
XM_024453005.1:c.1330G>A XP_024308773.1:p.Gly444Ser
XM_024453006.1:c.1267G>A XP_024308774.1:p.Gly423Ser
XR_001739705.1:n.3607-461C>T
XR_923313.2:n.4043-461C>T
NM_000312.4:c.1165G>A MANE Select NP_000303.1:p.Gly389Ser
NM_001375602.1:c.1348G>A NP_001362531.1:p.Gly450Ser
NM_001375603.1:c.1330G>A NP_001362532.1:p.Gly444Ser
NM_001375604.1:c.1228G>A NP_001362533.1:p.Gly410Ser
NM_001375605.1:c.1267G>A NP_001362534.1:p.Gly423Ser
NM_001375606.1:c.1333G>A NP_001362535.1:p.Gly445Ser
NM_001375607.1:c.1351G>A NP_001362536.1:p.Gly451Ser
NM_001375608.1:c.1108G>A NP_001362537.1:p.Gly370Ser
NM_001375609.1:c.1141G>A NP_001362538.1:p.Gly381Ser
NM_001375610.1:c.1159G>A NP_001362539.1:p.Gly387Ser
NM_001375611.1:c.1165G>A NP_001362540.1:p.Gly389Ser
NM_001375613.1:c.1165G>A NP_001362542.1:p.Gly389Ser
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